US3366704A - Ethylene polymerization to higher 1-olefins - Google Patents
Ethylene polymerization to higher 1-olefins Download PDFInfo
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- US3366704A US3366704A US420158A US42015864A US3366704A US 3366704 A US3366704 A US 3366704A US 420158 A US420158 A US 420158A US 42015864 A US42015864 A US 42015864A US 3366704 A US3366704 A US 3366704A
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/122—Metal aryl or alkyl compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
- C07C2/26—Catalytic processes with hydrides or organic compounds
- C07C2/30—Catalytic processes with hydrides or organic compounds containing metal-to-carbon bond; Metal hydrides
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/08—Halides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/08—Halides
- C07C2527/10—Chlorides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
Definitions
- This invention relates to a new process for the conversion of ethylene to higher, predominantly straight chain l-olefins.
- Straight chain olefins containing up to 20 carbon atoms are of particular interest at the present time as a raw material in the production of biodergradable detergents.
- the present invention is based upon the discovery of a new catalyst for the reaction.
- ethylene is converted to higher l-olefins, principally straight chain olefins, by contact, in a hydrocarbon diluent and at a pressure of at least 50 psi. and not more than 350 p.s.i., preferably not more than 300 p.s.i., above the vapor pressure of the diluent at the reaction temperature, with a product formed by mixing an organolithium compound with at least one compound selected from the group consisting of:
- the rare earth metals whose compounds are to be employed in the process of this invention are those having atomic numbers ranging from 57-71, inclusive, namely lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulim, ytterbium and lutetium.
- the halogens present in the halides and oxyhalides are chlorine, bromine and iodine.
- the catalyst systems of this invention will comprise an organolithium compound and at least one rare earth metal chloride, bromide, iodide, oxychloride, oxybromide or oxyiodide.
- rare earth metal compounds examples include lanthanum bromide, lanthanum chloride, lanthanum iodide, cerous chloride, cerous iodide, praseodymium bromide, praseodymium chloride, neodymium bromide, neodymium chloride, neodymium iodide, promethium chloride, samarium tribromide, samarium trichloride, samarium di- 3,366,704 Patented Jan.
- chloride samarium triodide, europium chloride, gadolini: um, gadolinium chloride, terbium chloride, dysprosium chloride, holmium chloride, erbium chloride, thulium chloride, ytterbium chloride, lutetium chloride, lanthanum oxybromide, lanthanum oxychloride, lanthanum oxyiodide, cerous oxychloride, ceric oxychloride, cerous oxyiodide, praseodymium oxybromide, praseodymium oxychloride, neodymium oxybromide, neodymium oxychloride, neodymium oxyiodide, promethium oxychloride, samarium oxybromide, samarium oxychloride, samarium oxyiodide, europium oxychloride,
- chlorides and/or oxychlorides of cerium are listed rare earth metal compounds. It is preferred to use chlorides and/or oxychlorides of cerium.
- the rare earth metal halides such as cerium trichloride
- the hydrated form Prior to utilizing such materials in the process of this invention, the hydrated form should be dehydrated before contacting the material with the organolithium reducing agents.
- the preferred method for effecting this dehydration is to heat under vacuum, although other methods, such as the treatment of the rare earth metal halide with thionyl chloride, can be employed.
- oxides examples include lanthanum oxide, cerous oxide, ceric oxide, praseodymium oxide, neodymium oxide, samarium oxide, europium oxide, gadolinium oxide, terbium oxide, dysprosium oxide, erbium oxide, thulium oxide and ytterbium oxide.
- the organolithium compounds which can be used are represented by the formula RLi wherein x is an integer of 1 to 4 and R is a hydrocarbon radical selected from the group consisting of aliphatic, cycloaliphatic, and aromatic radicals containing 1 to 20 carbon aotms.
- Preferred compounds have the formula RLi, wherein R is an alkyl, aryl, cycloalkyl, alkaryl or aralkyl radical containing not more than 10 carbon atoms. Mixed radicals are suitable.
- Specific examples of RM compounds include methyllithium,
- present during catalyst preparation generally ranges from 10 to 100 volume percent of the amount used in the ethylene conversion step.
- the amount of rare earth metal component present ranges l-lithio-4-(Z-lithiomethylphenyl)butane, 5 from to 100 millimoles per liter of reactor capacity, 1,2-di(lithiobutyl)benzene, while the mol ratio of RLi/rare earth metal compound 1,3-dilithio-4-ethylbenzene, generally ranges from 0.5/1 to 10/1.
- 1,5,IZ-trilithiododecane The polymerization can be carried out batchwise or 1,4-di(l,2-dilithio-2-phenylethyl)benzene, continuous, and reaction times can vary from a few minl,5-dilithio-3-pentyne, m utes to several hours.
- metal compounds can be used, e.g., alumina, silica, sil- 1,2-dilithiotriphenylethane, ica/ alumina, kieselguhr, etc.
- 1,4-di1ithio-1,1,4,4-t tr he 1b t catalyst system of this invention provides a new means 1,4-dilithi0-1,4-diphenyl-1,4-diuaphthylbutame, for converting ethylene to higher l-olefins of the straight 1,3,5-t 1ithio enta e, chain variety.
- the catalyst can be formed outside the vessel acid, the Solid Polymer recgve ed (if any present) by m Whloh y o 1S Converted t0 a blgber l'olofin and pouring into methanol and filtering, and the higher l-ole- Subsequently charged thereto, or the catalyst can be fins present analyzed by vapor phase chromatography. formed directly in the reaction vessel to which ethylene Th cerous hl id d i these runs h d been dehy 1810 be i drated by heating under a pressure of 1 mm.
- the dlluentemployed during catalyst p pa a i n is 40 for 4 hours at to 0., 4 hours at 100 to 200 0., mally the same diluent which is used when the catalyst is and 8 hours at 240 to 250.
- the polymerization is carried out at a temperature of The reactor efiluent from Run 2 was analyzed by VPC from about to P r y from to and found to contain olefins up through'C Fractionaat a Pressuro generally Tanglng from 100 to 1000 tion of the reactor efiluent yielded three fractions: p.s.i.g., preferably from 300 to 500 p.s.i.g. As described 65 above, the pressure employed should be at least 50 p.s.i. above and not more than 350 p.s.i. above, and preferably Fraction Volume, 1111. Boiling Range not more than 300 p.s.i. above, the vapor pressure of the diluent at the reaction temperature.
- the amount of hydrocarbon diluent present in the 're- A sample of fraction 3 was hydrogenated and then anaactor generally ranges from 50 to 500 cc. per liter of lyzed by VPC and found to be over 90 percent by weight polymerization reactor capacity.
- the amount of diluent 75 staright chain hydrocarbon.
- Infrared analysis of traction 3 showed predominantly l-olefins with small amounts of internal trans olefins present.
- the liquid product from Run 4 contained less C and higher olefins than in Run 2, but analysis indicated a higher percentage of branched materials were produced. This indicates that higher temperatures cause more branching to occur.
- Run 5 illustrates polymerization substantially like Run 4 but at a diflferent catalyst ratio.
- Run 6 shows that low temperatures should be avoided as well as excessive pres-sure when liquid products are desired.
- a process of converting ethylene to higher predominantly straight chain l-olefins comprising contacting ethylene in hydrocarbon diluent with a rare earth metal-organolithium catalyst which forms on mixing (a) at least one compound selected from the group consisting of:
- the mixture contains at least 5 weight percent halogen; and (b) at least one organolithium compound of the formula RLi where x is an integer from 1 to 4 and R is a hydrocarbon radical selected from the group consisting of aliphatic, cycloaliphatic and aromatic radicals containing not more than carbon atoms, at a pressure at least 50 but not more than 350 psi. above the vapor pressure of the diluent at the reaction temperature and the mole ratio of said organolithium compound to rare earth metal component being from 05/1 to 10/1.
- a process of converting ethylene to higher predominantly straight chain l-olefins comprising contacting ethylene in hydrocarbon diluent with a rare earth metal-organolithium catalyst which forms on mixing (a) at least one compound selected from the group consisting of:
- the mixture contains at least 5 weight percent halogen, and (b) at least one compound of the formula RLi wherein R is selected from the group consisting of alkyl, aryl, cycloalkyl, aralkyl and alkaryl radicals containing not more than 10 carbon atoms at a pressure at least 50 but not more than 350 p.s.i. above the vapor pressure of the diluent at the reaction temperature and the mole ratio of said organolithium compound to rare earth metal component being from 0.5/1 to 10/1.
- a process of converting ethylene to higher predominantly straight chain l-olefins containing 6 to 20 carbon atoms comprising contacting ethylene in an aromatic hydrocarbon diluent with a catalyst which forms on mixing cerous chloride and butyllithium at a pressure at least 50 but not more than 300 p.s.i. above the vapor pressure of the diluent at the reaction, temperature.
- a process for polymerizing ethylene to higher predominantly straight chain l-olefins containing up to 20 carbon atoms comprising contacting ethylene in'aromatic hydrocarbon diluent at a temperature of to 300 C. and at a pressure at least 50 psi. and not more than 300 psi. above the vapor pressure of the diluent at the reaction temperature with a catalyst which forms on mixing butyllithium and cerous chloride, said catalyst components having been mixed in the absence of ethylene and heated to a temperature of 100 to 225 C.
- chloride read chlorides read chlorides, bromides, and
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Description
United States Patent 3,366,704 ETHYLENE POLYMERIZATION TO HIGHER I-OLEFINS Paul R. Stapp, Bartlesville, 0kla., assignor to Phillips Petroleum Company, a corporation of Delaware N0 Drawing. Filed Dec. 21, 1964, Ser. No. 420,158 8 Claims. (Cl. 260-68315) ABSTRACT OF THE DISCLOSURE Ethylene is converted to higher l-olefins, principally straight chain olefins, by contact in a hydrocarbon diluent and at a pressure of at least 50 psi. and not more than 350 -p.s.i. above the vapor pressure of the diluent at the reaction temperature, with a product formed by mixing an organolithium compound and at least one compound selected from the group consisting of: (l) rare earth metal chlorides, bromides, and iodides; (2) rare earth metal oxychlorides, oxybromi-des, and oxyiodides; (3) mixtures of (1) and (2); or (4) mixtures of at least one of (1) and (2) with a rare earth metal oxide wherein the mixture contains at least 5 Weight percent halogen.
This invention relates to a new process for the conversion of ethylene to higher, predominantly straight chain l-olefins. Straight chain olefins containing up to 20 carbon atoms are of particular interest at the present time as a raw material in the production of biodergradable detergents. The present invention is based upon the discovery of a new catalyst for the reaction.
It is therefore the object of this invention to provide a new process for the production of straight chain l-olefins from ethylene and, further, to minimize coproduction of branched olefins in such a process.
According to the process of this invention, ethylene is converted to higher l-olefins, principally straight chain olefins, by contact, in a hydrocarbon diluent and at a pressure of at least 50 psi. and not more than 350 p.s.i., preferably not more than 300 p.s.i., above the vapor pressure of the diluent at the reaction temperature, with a product formed by mixing an organolithium compound with at least one compound selected from the group consisting of:
(1) rare earth metal halides,
(2) rare earth metal oxyhalides,
(3) mixtures of (1) and (2), and
(4) mixtures of at least one of (1) and (2) with a rare earth metal oxide wherein the mixture contains at least 5 weight percent halogen.
The rare earth metals whose compounds are to be employed in the process of this invention are those having atomic numbers ranging from 57-71, inclusive, namely lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulim, ytterbium and lutetium.
As used herein, the halogens present in the halides and oxyhalides are chlorine, bromine and iodine. Thus, the catalyst systems of this invention will comprise an organolithium compound and at least one rare earth metal chloride, bromide, iodide, oxychloride, oxybromide or oxyiodide.
Examples of the rare earth metal compounds are lanthanum bromide, lanthanum chloride, lanthanum iodide, cerous chloride, cerous iodide, praseodymium bromide, praseodymium chloride, neodymium bromide, neodymium chloride, neodymium iodide, promethium chloride, samarium tribromide, samarium trichloride, samarium di- 3,366,704 Patented Jan. 30, 1968 chloride, samarium triodide, europium chloride, gadolini: um, gadolinium chloride, terbium chloride, dysprosium chloride, holmium chloride, erbium chloride, thulium chloride, ytterbium chloride, lutetium chloride, lanthanum oxybromide, lanthanum oxychloride, lanthanum oxyiodide, cerous oxychloride, ceric oxychloride, cerous oxyiodide, praseodymium oxybromide, praseodymium oxychloride, neodymium oxybromide, neodymium oxychloride, neodymium oxyiodide, promethium oxychloride, samarium oxybromide, samarium oxychloride, samarium oxyiodide, europium oxychloride, gadolinium oxybromide, gadolinium oxychloride, terbium oxychloride, dysprosium oxychloride, holmium oxychloride, erbium oxychloride, thulium oxychloride, ytterium oxychloride, and lutetium oxychloride. Halides of mixtures of rare earths, e.g. didymium, chloride, can be employed if desired.
Of the listed rare earth metal compounds, it is preferred to use chlorides and/or oxychlorides of cerium.
Several of the rare earth metal halides, such as cerium trichloride, are normally obtained commercially in a hydrated form. Prior to utilizing such materials in the process of this invention, the hydrated form should be dehydrated before contacting the material with the organolithium reducing agents. The preferred method for effecting this dehydration is to heat under vacuum, although other methods, such as the treatment of the rare earth metal halide with thionyl chloride, can be employed.
Examples of the oxides include lanthanum oxide, cerous oxide, ceric oxide, praseodymium oxide, neodymium oxide, samarium oxide, europium oxide, gadolinium oxide, terbium oxide, dysprosium oxide, erbium oxide, thulium oxide and ytterbium oxide.
The organolithium compounds which can be used are represented by the formula RLi wherein x is an integer of 1 to 4 and R is a hydrocarbon radical selected from the group consisting of aliphatic, cycloaliphatic, and aromatic radicals containing 1 to 20 carbon aotms. Preferred compounds have the formula RLi, wherein R is an alkyl, aryl, cycloalkyl, alkaryl or aralkyl radical containing not more than 10 carbon atoms. Mixed radicals are suitable. Specific examples of RM compounds include methyllithium,
n-butyllithium, sec-butyllithium, tert-butyllithium, Z-butenyllithium, isooctyllithium, n-decyllithium,
phenyllithium, cyclohexyllithiurn, 2-cyclohexenyllithium, naphthyllithium, 4-n-butylphenyllithium, benzyllithium, 4-phenylbutyllithium, 4-phenylhexadecyllithium, 1,4-dilithiobutane, 1,6-dilithiohexane, 1,10-dilithiodecane, 1,20-dilithioeicosane, 1,4-dilithio-2-methyl-2-butene, 1,4-dilithio-2-butene, dilithionaphthalene, dilithiometh-ylnaphthalene, 4,4'-dilithiobiphenyl, dilithioanthracene,
l, l-dilithio-l l-di-phenylethane, 1,2-dilithio-1,2-diphenylethane, l,2-dilithiotetraphenylethane, 1,2-dilithio-1-phenyl-l-naphthylethane,
. 3 1,2-dilithio-1,Z-dinaphthylethane, 1,2-dilithiotrinaphthylethane, 1,4-dilithiocyclohexane,
1,3 ,5 -trilithiocyclohexane,
present during catalyst preparation, if a separate step is used, generally ranges from 10 to 100 volume percent of the amount used in the ethylene conversion step. The amount of rare earth metal component present ranges l-lithio-4-(Z-lithiomethylphenyl)butane, 5 from to 100 millimoles per liter of reactor capacity, 1,2-di(lithiobutyl)benzene, while the mol ratio of RLi/rare earth metal compound 1,3-dilithio-4-ethylbenzene, generally ranges from 0.5/1 to 10/1. 1,5,IZ-trilithiododecane, The polymerization can be carried out batchwise or 1,4-di(l,2-dilithio-2-phenylethyl)benzene, continuous, and reaction times can vary from a few minl,5-dilithio-3-pentyne, m utes to several hours. Inert supports for the rare earth dilithiophenanthrene, metal compounds can be used, e.g., alumina, silica, sil- 1,2-dilithiotriphenylethane, ica/ alumina, kieselguhr, etc. dilithiomethane, The following specific example clearly shows that the 1,4-di1ithio-1,1,4,4-t tr he 1b t catalyst system of this invention provides a new means 1,4-dilithi0-1,4-diphenyl-1,4-diuaphthylbutame, for converting ethylene to higher l-olefins of the straight 1,3,5-t 1ithio enta e, chain variety. The example should not be considered un- 2,4,-6-trilithiooctane-2, y limiting- 1,4,S-trilithionaphthalene, 4,8, 12-trilithioeicosane, EXAMPLE 3 5 9 i1i hi g h l d A series of runs was carried out in which the reaction 2 4 i1i hi product of cerous chloride (CeCl and butyllithium was 2,3,4,54etra1ithiooctane, employed for the conversion of ethylene to higher 1- 2,3,4,5-tetralithiononene-1, Olefins' 35,7,9 tetra1ithioeicosane In each of these runs, the n-butyllithium and the cerous 2,3,7,3,tetralithio 6 n decy1naphtha1ene chloride werecharged to a 1-liter autoclave along with 2,4,684etralithiocw1ododecane and the like. 200 ml. of diluent and heated to a temperature in the range 100 to 225 C. in the absence of ethylene, after The active catalyst for the conversion of ethyl n which ethylene was pressured into the reactor to a preshlgbfif Straight oballl 1-o1ofin$ 15 formed y mlxmg b sure in the range 175 to 500 p.s.i.g. The addition of ethyleanh metal Compound wlthfho x compound In one was continued on an open valve to maintain the prestho Presence of a hydrocarbon dlhlont- Mlxturbs of two sure at the initial pressure, and each run was carried out more rare earth metal Compounds and two more for a time of 3.25 to 4.0 hours. The reactor was then ix compounds can be Used- The Components generally cooled and vented, the reactor effluent removed and hyreact at room temperature, but elevated temperatures can d l d i dilute aqueous hydrochloric of Sulfuric be employed. The catalyst can be formed outside the vessel acid, the Solid Polymer recgve ed (if any present) by m Whloh y o 1S Converted t0 a blgber l'olofin and pouring into methanol and filtering, and the higher l-ole- Subsequently charged thereto, or the catalyst can be fins present analyzed by vapor phase chromatography. formed directly in the reaction vessel to which ethylene Th cerous hl id d i these runs h d been dehy 1810 be i drated by heating under a pressure of 1 mm. Hg absolute The dlluentemployed during catalyst p pa a i n is 40 for 4 hours at to 0., 4 hours at 100 to 200 0., mally the same diluent which is used when the catalyst is and 8 hours at 240 to 250. The butyllithium used in contacted With thyl H W ver, different diluents can these runs was charged as a 1.56 molar solution in hexane. be used in these two steps. Suitable diluents include hydro- Results are shown in the following table.
Pressure Run Dilueut iiili i l t li il fii Temp.,C. i g ng 53135 Results p.s.i. diluent,
1 Xylene 200 40 175 *175 130-145 3.25 Smallgmouut solid polymer, more iqui 33:11:: j i ir iiifjjjilii 53% 33 it 333 it?) it? i it'gr rts sii ffrrit.i ofl ts(s... to 4 do 200 40 120 225 315 98 4 75 ilir'ss liquid olefius. 2111;11:11113311111111: 53% i3 13% it?) 450-23?) mitt i h$sitit fitiiiir siiif carbons Such as heptane, hexane, octane, benzene, toluene, In Run 1 vapor phase chromatographic analysis (VPC) y deoalin, oyolohexane, oyoloootabo, mothyloyolo- 60 of the liquid product showed the presence of l-hexene, hexane, and the likel-octene and l-dodecene.
The polymerization is carried out at a temperature of The reactor efiluent from Run 2 was analyzed by VPC from about to P r y from to and found to contain olefins up through'C Fractionaat a Pressuro generally Tanglng from 100 to 1000 tion of the reactor efiluent yielded three fractions: p.s.i.g., preferably from 300 to 500 p.s.i.g. As described 65 above, the pressure employed should be at least 50 p.s.i. above and not more than 350 p.s.i. above, and preferably Fraction Volume, 1111. Boiling Range not more than 300 p.s.i. above, the vapor pressure of the diluent at the reaction temperature. If higher pressures 1 60 2570 C. at atm. are employed, higher concentrations of ethylene will be 70 gIZIIIIIII: 33359353 23 5%: g? present in the reaction zone, and this will lead to increased formation of solid ethylene polymer.
The amount of hydrocarbon diluent present in the 're- A sample of fraction 3 was hydrogenated and then anaactor generally ranges from 50 to 500 cc. per liter of lyzed by VPC and found to be over 90 percent by weight polymerization reactor capacity. The amount of diluent 75 staright chain hydrocarbon. Infrared analysis of traction 3 showed predominantly l-olefins with small amounts of internal trans olefins present.
Distillation of the liquid product from Run 3 gave m1. of olefins boiling at 2674 C. at 22 mm. Hg and 26 ml. of olefins boiling at 85-175 C. at 15-2 mm. Hg.
The liquid product from Run 4 contained less C and higher olefins than in Run 2, but analysis indicated a higher percentage of branched materials were produced. This indicates that higher temperatures cause more branching to occur. Run 5 illustrates polymerization substantially like Run 4 but at a diflferent catalyst ratio. Run 6 shows that low temperatures should be avoided as well as excessive pres-sure when liquid products are desired.
Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of the invention, and it should be understood that the latter is not necessarily limited to the aforementioned discussion.
That which is claimed is:
1. A process of converting ethylene to higher predominantly straight chain l-olefins comprising contacting ethylene in hydrocarbon diluent with a rare earth metal-organolithium catalyst which forms on mixing (a) at least one compound selected from the group consisting of:
(1) rare earth metal chloride, bromides, and iodides,
(2) rare earth metal oxychlorides, oxybromides, and
oxyiodides,
(3) mixtures of (1) and (2), and
(4) mixtures of at least one of (1) and (2) with a rare earth metal oxide,
wherein the mixture contains at least 5 weight percent halogen; and (b) at least one organolithium compound of the formula RLi where x is an integer from 1 to 4 and R is a hydrocarbon radical selected from the group consisting of aliphatic, cycloaliphatic and aromatic radicals containing not more than carbon atoms, at a pressure at least 50 but not more than 350 psi. above the vapor pressure of the diluent at the reaction temperature and the mole ratio of said organolithium compound to rare earth metal component being from 05/1 to 10/1.
2. A process of converting ethylene to higher predominantly straight chain l-olefins comprising contacting ethylene in hydrocarbon diluent with a rare earth metal-organolithium catalyst which forms on mixing (a) at least one compound selected from the group consisting of:
(1) rare earth metal halides,
(2) rare earth metal oxyhalides,
(3) mixtures of (1) and (2), and
(4) mixtures of at least one of (1) and (2) with a rare earth metal oxide,
wherein the mixture contains at least 5 weight percent halogen, and (b) at least one compound of the formula RLi wherein R is selected from the group consisting of alkyl, aryl, cycloalkyl, aralkyl and alkaryl radicals containing not more than 10 carbon atoms at a pressure at least 50 but not more than 350 p.s.i. above the vapor pressure of the diluent at the reaction temperature and the mole ratio of said organolithium compound to rare earth metal component being from 0.5/1 to 10/1.
3. The process of claim 2 wherein said contacting is carried out at 160 to 300 C. at a pressure of to 1000 p.s.i.g.
4. The process of claim 3 wherein the amount of rare earth metal component is in the range of 10 to 100 millimoles'per liter of reactor capacity.
5. A process of converting ethylene to higher predominantly straight chain l-olefins containing 6 to 20 carbon atoms comprising contacting ethylene in an aromatic hydrocarbon diluent with a catalyst which forms on mixing cerous chloride and butyllithium at a pressure at least 50 but not more than 300 p.s.i. above the vapor pressure of the diluent at the reaction, temperature.
6. The process of claim 5 wherein said diluent is selected from the group consisting of xylene and benzene.
7. A process for polymerizing ethylene to higher predominantly straight chain l-olefins containing up to 20 carbon atoms comprising contacting ethylene in'aromatic hydrocarbon diluent at a temperature of to 300 C. and at a pressure at least 50 psi. and not more than 300 psi. above the vapor pressure of the diluent at the reaction temperature with a catalyst which forms on mixing butyllithium and cerous chloride, said catalyst components having been mixed in the absence of ethylene and heated to a temperature of 100 to 225 C.
8. The process of claim 7 wherein the amount of cerous chloride is 10-100 millimoles per liter of reactor capacity I and the mole ratio of butyllithium to cerous chloride is in the range of 0.5/1 to 10/1.
References Cited UNITED STATES PATENTS PAUL M. COUGHLAN, JR., Primary Examiner.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No 3 ,366 ,704 January 30 1968 Paul R. Stapp that error appears in the above numbered pat- It is hereby certified d that the said Letters Patent should read as ent requiring correction an corrected below.
for "chloride" read chlorides read chlorides, bromides, and
" read oxychlorides,
oxybromides, and oxyiodides Signed and sealed this 3rd day of June 1969.
Edward M. Fletcher, Jr.
Commissioner of Patents Attesting Officer
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US420158A US3366704A (en) | 1964-12-21 | 1964-12-21 | Ethylene polymerization to higher 1-olefins |
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US420158A US3366704A (en) | 1964-12-21 | 1964-12-21 | Ethylene polymerization to higher 1-olefins |
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US3366704A true US3366704A (en) | 1968-01-30 |
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US420158A Expired - Lifetime US3366704A (en) | 1964-12-21 | 1964-12-21 | Ethylene polymerization to higher 1-olefins |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4482640A (en) * | 1983-05-02 | 1984-11-13 | Phillips Petroleum Company | Ethylene oligomerization |
US4518814A (en) * | 1983-05-02 | 1985-05-21 | Phillips Petroleum Company | Ethylene oligomeration |
US4801666A (en) * | 1985-03-25 | 1989-01-31 | Northwestern University | Olefin and cycloalkene polymerization with organolanthanide catalysts |
Citations (6)
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---|---|---|---|---|
US2921060A (en) * | 1956-07-12 | 1960-01-12 | Sun Oil Co | Polymerization of ethylene with a cerium acetylacetonate-metal alkyl catalyst |
US2953531A (en) * | 1954-08-16 | 1960-09-20 | Du Pont | Cerium polymerization catalysts |
US3056770A (en) * | 1958-03-04 | 1962-10-02 | Dal Mon Research Co | Polymerization process |
US3111511A (en) * | 1959-04-06 | 1963-11-19 | Grace W R & Co | Polymerization of ethylene with aluminum alkyl-rare earth halide catalysts |
US3125559A (en) * | 1964-03-17 | Process for polymerizing unsaturated | ||
US3179647A (en) * | 1957-02-07 | 1965-04-20 | Ici Ltd | Polymerisation catalysts consisting of an aluminum alkyl and a rare earth metal chloride or oxide |
-
1964
- 1964-12-21 US US420158A patent/US3366704A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US3125559A (en) * | 1964-03-17 | Process for polymerizing unsaturated | ||
US2953531A (en) * | 1954-08-16 | 1960-09-20 | Du Pont | Cerium polymerization catalysts |
US2921060A (en) * | 1956-07-12 | 1960-01-12 | Sun Oil Co | Polymerization of ethylene with a cerium acetylacetonate-metal alkyl catalyst |
US3179647A (en) * | 1957-02-07 | 1965-04-20 | Ici Ltd | Polymerisation catalysts consisting of an aluminum alkyl and a rare earth metal chloride or oxide |
US3056770A (en) * | 1958-03-04 | 1962-10-02 | Dal Mon Research Co | Polymerization process |
US3111511A (en) * | 1959-04-06 | 1963-11-19 | Grace W R & Co | Polymerization of ethylene with aluminum alkyl-rare earth halide catalysts |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4482640A (en) * | 1983-05-02 | 1984-11-13 | Phillips Petroleum Company | Ethylene oligomerization |
US4518814A (en) * | 1983-05-02 | 1985-05-21 | Phillips Petroleum Company | Ethylene oligomeration |
US4801666A (en) * | 1985-03-25 | 1989-01-31 | Northwestern University | Olefin and cycloalkene polymerization with organolanthanide catalysts |
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